Blank M L, Fitzgerald V, Smith Z L, Snyder F
Medical Sciences Division, Oak Ridge Associated Universities, Tennessee 37831-0117, USA.
Biochem Biophys Res Commun. 1995 May 25;210(3):1052-8. doi: 10.1006/bbrc.1995.1763.
The microsomal fraction from rat spleen was shown to possess a CoA-dependent transacylase activity that produced 1-[3H]alkyl-2-lyso-sn-glycero-3-phosphocholine ([3H]lyso-PAF), the immediate precursor of PAF in the remodeling pathway of biosynthesis, from 1-[3H]alkyl-2-acyl-sn-glycero-3-phosphocholine. This CoA-dependent transacylase did not require ATP or metal ions for activity making it unlikely that either acyl-CoA-synthetase or a Ca(2+)-dependent phospholipase A2 were involved in the generation of [3H]lyso-PAF. Albumin, in addition to CoA, was required to demonstrate the formation of [3H]lyso-PAF from 1-[3H]alkyl-2-acyl-sn-glycero-3-phosphocholine. It appeared that a major function of albumin in the incubations was to complex the [3H]lyso-PAF formed, thus removing this end-product from the reaction.
大鼠脾脏微粒体部分被证明具有一种依赖辅酶A的转酰基酶活性,该活性可从1-[³H]烷基-2-酰基-sn-甘油-3-磷酸胆碱产生1-[³H]烷基-2-溶血-sn-甘油-3-磷酸胆碱([³H]溶血血小板活化因子),它是生物合成重塑途径中血小板活化因子的直接前体。这种依赖辅酶A的转酰基酶活性不需要ATP或金属离子,这使得酰基辅酶A合成酶或钙依赖性磷脂酶A2不太可能参与[³H]溶血血小板活化因子的生成。除了辅酶A外,还需要白蛋白来证明从1-[³H]烷基-2-酰基-sn-甘油-3-磷酸胆碱形成[³H]溶血血小板活化因子。在孵育过程中,白蛋白的主要功能似乎是与形成的[³H]溶血血小板活化因子结合,从而将该终产物从反应中去除。